Viewing Study NCT05852236



Ignite Creation Date: 2024-05-06 @ 6:59 PM
Last Modification Date: 2024-10-26 @ 2:58 PM
Study NCT ID: NCT05852236
Status: COMPLETED
Last Update Posted: 2023-05-10
First Post: 2023-04-04

Brief Title: The Effect of Pressure Wound Care Package on the Development of Operating Room Pressure Wound in Orthopedic Surgery
Sponsor: Sehitkamil Devlet Hastanesi
Organization: Sehitkamil Devlet Hastanesi

Study Overview

Official Title: The Effect of Pressure Wound Care Package on OR Pressure Wound Development
Status: COMPLETED
Status Verified Date: 2023-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: SUMMARY In a non-randomised quasi-experimental clinical study it was aimed to determine the effect of the care package applied in the early postoperative period on operating theatre pressure sores pain fear of falling and comfort in patients undergoing orthopaedic surgery In the study the care bundle for pressure injuries was prepared in accordance with the clinical guidelines and was applied to the patients in the study group This study was conducted in the orthopaedics and traumatology clinic of a public hospital in the Southeastern Anatolia Region of Turkey
Detailed Description: MedhodPatients in the control group underwent routine practice of the clinic and this group was observed for 199 days The care bundle for pressure injuries developed within the scope of the research was not applied In the study group in addition to routine clinical practice the care bundle for pressure injuries developed for this study was applied for 105 days Since the pressure ulcer originating from the operating room was seen until the 48th-72nd hour the evaluations and interventions within the scope of the study were performed for three days considering the operation day as the zeroth day for the control and study groups A total of 190 patients 122 in the control group and 68 in the study group were included in the study

The care bundle consisted of skin care positioning early mobilization nutrition and fluid intake interventions In the study first the data of the control group and then the data of the study group were collected

Data Collection Tools The Patient Descriptive Information Form consists of sociodemographic data The 3S OR Pressure Injury Risk Assessment Scale was used to identify patients at risk of developing OR pressure ulcers Visual Analogue Scale was used to evaluate pain perception The Visual Analog Scale was used to determine the fear of falling General Comfort Questionnaire-Short Form was used to determine the comfort level The National Pressure Ulcer Advisory Panel NPUAP 2016 Pressure Injury Staging System was used to assess and stage pressure ulcer development Pressure Injury Areas and Stages Follow-up Registration Form The form in which the pressure ulcer development status is recorded

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None